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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5196Erstellt: 25. Oktober 2026

Diisopropylamine → Ethyl 2-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/5196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Methyl-4-(2-nitroethenyl)benzeneHCID 286735—
EduktEthyl(diethoxymethyl)methylphosphinateHCID 13764418—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktEthyl 2-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinateHCID 14362829—

Reaktionsschritte

To a solution of 8.7 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 53.6 ml of a 1.6M solution of n-butyllithium in hexane. This solution is then stirred for a period of 10 minutes at this temperature, after which time a solution of 15.0 g of ethyl(diethoxymethyl)methylphosphinate in 20 ml of tetrahydrofuran is added. This mixture is then stirred for a period of 1 hour at -78° C. after which time a solution of 11.6 g of 4-methyl-β-nitrostyrene in 20 ml of tetrahydrofuran is introduced. This mixture is then allowed to warm to room temperature when 40 ml of a saturated ammonium chloride solution is added. The aqueous layer is then extracted with 2×25 ml of diethyl ether and the organic extracts are combined and dried over magnesium sulphate. The solvent is then evaporated under reduced pressure and the crude product chromatographed on silica gel using ethyl acetate as an eluent to give ethyl 2-(4-methylphenyl)-3-nitropropyl(diethoxymethyl)phosphinate as a viscous oil, 31 p=+42.5 and +42.1 ppm (CDCl3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05243062
Quelldatensatzuspto-grants-1993_09
ORD IDord-789e38ffe1424cb886e603ae877f3048
Quellennotizuspto-grants-1993_09